sanofi-aventis Korea Co., Ltd. Posted October 2, 2026

Quality Associate

Seoul, South Korea Full time
Quality Associate
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sanofi-aventis Korea Co., Ltd. is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Job title: Quality Associate

 

●         Location: Seoul, South Korea

* This is a 1.5 year temporary position.

About the job

About Sanofi:

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

Main responsibilities:

Manage product technical complaints, monitor investigation activities, and follow up on outcomes to ensure timely resolution.

Handle quality events, including deviations, change controls, and CAPA activities.

Coordinate and support analytical method validation and transfer activities to ensure timely and successful implementation.

Maintain quality agreements with manufacturing sites and third-party suppliers of products and reference standards.

Support product release activities in compliance with local regulatory requirements and company quality standards.

Maintain quality documentation and training records, ensuring they remain accurate and up to date.

Support the delivery and tracking of GMP and quality-related training activities across the team.

Support quality audits and inspections, including self-inspections, MFDS overseas GMP inspections, MFDS GIP inspections, and health authority inspections.

Follow up on inspection observations and corrective and preventive actions (CAPAs) to ensure timely closure.

Liaise with local health authorities regarding quality-related regulatory requests and commitments.

Serve as backup for Annual Product Quality Review (APQR) activities.

About you

Experience: Background in pharmaceutical quality assurance, quality control, or regulatory affairs(2-5 years of relevant experience required)

Soft and technical skills: Strong attention to detail, analytical thinking, and familiarity with GxP quality systems and complaint/deviation handling processes; able to work independently and collaboratively across cross-functional teams

Education: Degree in Pharmacy, Chemistry, Life Sciences, or a related field

Languages: Professional proficiency in English for collaboration with global teams

Why choose us?

Help shape the future of care for chronic and complex conditions like aT1D, Type 2 diabetes, transplant, and cardiovascular disease.

Drive meaningful impact at global scale: our medicines reach more than 100 million people each year.

Be part of a simpler, digital- and AI-powered business that’s rethinking how we work and engage with the world.

Turn bold ideas into breakthrough launches, with multiple new therapies planned through 2030 and beyond.

Stretch your career in a development playground, with opportunities across functions, regions, and the entire product lifecycle.

Pursue progress , discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com !

Job details

Seniority
Associate
Function
Quality
Therapeutic area
Not listed
Location
Seoul, South Korea
Employment type
Full time

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 385 comparable Associate Quality roles across 89 biopharma companies.

385Comparable roles tracked
347Currently active
89Companies hiring similar roles
37Countries represented

Salary context

44 of 385 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Associate I, Quality Control, Raw Materials · ModernaTX, Inc. $53,500/yr – $85,600/yr
Peer group range $69,550 – $190,750 (median $156,000)

Where these roles are based

Top locations among the 385 comparable roles

United States124
Germany40
France38
India28
China24
Ireland22

+ 31 more countries

Seniority mix

385 of 385 peers have a known seniority level

Manager223
Intern/Fellow/Postdoc98
Associate64

Therapeutic area mix

1 of 385 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Respiratory1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

50%similar
Merck KGaA Ansan-Si, Gyeonggi-do, Korea (the Republic of) Manager
Same function Adjacent seniority Same country
45%similar
Merck KGaA Milwaukee, Wisconsin, United States Associate
Same function Same seniority
45%similar
CSL Behring L.L.C. Seqirus USA - MA - Waltham, United States Associate
Same function Same seniority
45%similar
Devens Devens, United States Associate
Same function Same seniority
45%similar
BMS Netherlands Operations B.V. Leiden – NL, Netherlands Associate
Same function Same seniority
45%similar
Moderna Biotech Spain S.L.U. Madrid, Spain Associate
Same function Same seniority

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Quality job in South Korea, and choose locations and companies.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

50%
Regional Equipment Quality Manager (8년 이상, 팀 리딩_리더십)
Merck KGaA · Ansan-Si, Gyeonggi-do, Korea (the Republic of) · Manager
Function Therapeutic area Adjacent seniority Country
45%
Associate, QC Analytical, Cell Therapy
Devens · Devens, United States · Associate
Function Therapeutic area Seniority Country
45%
QA Associate
BioMarin Pharmaceutical Inc. · Cork, Ireland · Associate
Function Therapeutic area Seniority Country
45%
QS&C Associate Manager_System Digitalization
Roche · Shanghai, Shanghai, China's Mainland · Associate
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.